FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ETCHING GEL

K Number: K810266 · Decision Feb 23, 1981
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
76
Applicant Total
10
Review Days
21

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Basic Information

Device Name
ETCHING GEL
K Number
K810266
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3250
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Espe-Premier Sales Co.
Date Received
February 2, 1981
Decision Date
February 23, 1981
Product Code
EJK
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EJK Liner, Cavity, Calcium Hydroxide

Similar 510(k) Clearances

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Other Clearances by Espe-Premier Sales Co.

K Number Device Name
K812117 PERMAGUM ADHESIVE
K812116 PERMAGUM
K812115 KETAC-CHEM
K812118 NIMETIC POLISHING PASTE
K812119 NIMETIC-DISPERS
K811624 VISIO-SEAL
K810265 VISIO-BAND
K803227 VISIO-DISPERS
K803209 ELIPAR LIGHT SOURCE